Teams at Rhythm Pharmaceuticals

Manages scientific publication activities across integrated publication plans, coordinating authors, vendors, internal stakeholders, submissions, documentation, timelines, budgets, and congress materials. Ensures compliance with publication standards, maintains accurate records, tracks milestones, resolves operational issues, and improves processes. The role supports medical affairs and publication teams in a pharmaceutical environment.

Provides statistical programming support for clinical studies, regulatory submissions, and integrated analyses. Develops, validates, and maintains ADaM datasets, tables, listings, figures, specifications, macros, and submission documentation using SAS and CDISC standards. Partners with cross-functional teams and vendors, supports submission readiness, resolves programming risks, improves processes, and may mentor programmers, oversee vendors, and contribute to departmental standards.

Develop, validate, and QC analysis datasets, tables, listings, and figures for clinical studies and regulatory submissions. Create ADaM specs, TLF shells, reusable macros, and submission-ready documentation (define.xml, reviewer guides). Partner with Biostatistics, Data Management, Clinical Development, and vendors; identify risks, drive process improvements, and mentor junior programmers as needed.